Evidence map›Paper›PMID 24517394›Full record

ArticleBMC cell biology2014

Hepatic progenitor cells express SerpinB3.

Gianmarco Villano, Cristian Turato, Santina Quarta, Mariagrazia Ruvoletto, Francesco Ciscato, Liliana Terrin, Rossella Semeraro, Claudia Paternostro, Maurizio Parola, Domenico Alvaro and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. The protease-inhibitor SerpinB3 as a critical modulator of the stem-like subset in human cholangiocarcinoma.Liver international : official journal of the International Association for the Study of the Liver · 2022
    Article
  5. Engineered EVs for Oxidative Stress Protection.Pharmaceuticals (Basel, Switzerland) · 2021
    Article
  6. Article
  7. The diversity and plasticity of adult hepatic progenitor cells and their niche.Liver international : official journal of the International Association for the Study of the Liver · 2017
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. SERPINB3 (serpin peptidase inhibitor, clade B (ovalbumin), member 3).Atlas of genetics and cytogenetics in oncology and haematology
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Gianmarco Villano
Cristian Turato
Santina Quarta
Mariagrazia Ruvoletto
Francesco Ciscato
Liliana Terrin
Rossella Semeraro
Claudia Paternostro
Maurizio Parola
Domenico Alvaro
Paolo Bernardi
Angelo Gatta
Patrizia PontissoDepartment of Medicine-DIMED, University of Padua, Via Giustiniani 2, Padua 35128, Italy. patrizia@unipd.it.
University of Padua · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn the setting of liver injury hepatic progenitor cells are activated, counterbalancing the inhibited regenerative capacity of mature hepatocytes. Chronic activation of this compartment may give rise to a subset of liver tumours with poor prognosis. SerpinB3, a serpin over-expressed in injured liver and in primary liver cancer, has been shown to induce apoptosis resistance, epithelial to mesenchymal transition and to increase TGF-beta and Myc expression. Aim of the present study was to explore the presence of SerpinB3 in hepatic progenitor cells in human livers and in a mouse model of liver stem/progenitor cell activation.Hepatic progenitor cells were analysed in foetal and adult livers at protein and transcriptional levels. To induce experimental activation of the liver stem/progenitor compartment, C57BL/6J mice were injected with lipopolysaccharide plus D-galactosamine and were sacrificed at different time points. Liver cDNA was amplified using specific primers for mouse-homologous SerpinB3 isoforms and automatically sequenced.

resultsThe presence of SerpinB3 in the progenitor cell compartment was detected in sorted human foetal and adult epithelial cell adhesion molecule (EpCAM) positive liver cells. By immunohistochemistry SerpinB3 was found in human cirrhotic livers in portal areas with progenitor cell activation showing ductular proliferation. CK-7, CK-19, EpCAM and CD-90 positive cell were also positive for SerpinB3. In the animal model, time course analysis in liver specimens revealed a progressive increase of SerpinB3 and a parallel decrease of activated caspase 3, which was barely detectable at 20 hours. Transcription analysis confirmed the presence of SerpinB3-homologous only in the liver of injured mice and sequence analysis proved its belonging to mouse Serpinb3b.

conclusionSerpinB3 is highly expressed in hepatic stem/progenitor cell compartment of both foetal and adult livers.

Indexed as

AnimalsAntigens, NeoplasmBase SequenceCaspase 3Cell Adhesion MoleculesDisease Models, AnimalEpithelial Cell Adhesion MoleculeHumansImmunohistochemistryKeratin-19Keratin-7LiverLiver CirrhosisMiceMice, Inbred C57BLMolecular Sequence DataAntigens, NeoplasmCaspase 3Cell Adhesion MoleculesEpithelial Cell Adhesion MoleculeKeratin-19Keratin-7Serpinssquamous cell carcinoma-related antigenThy-1 Antigens

Identifiers

PMID24517394
PMCPMC3927218
OpenAlexW1966829944

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.